ClinicalTrials.gov Registration User s Guide. January 2018

Transcription

1 ClinicalTrials.gov Registration User s Guide January 2018

2 ClinicalTrials.gov Assistance and Training at WCM Contact the WCM ClinicalTrials.gov Administrator at to: Schedule a one on one to review these slides and ClinicalTrials.gov responsibilities Obtain a ClinicalTrials.gov account for yourself or a designee Visit the WCM ClinicalTrials.gov site at otgov.html

3 Caveats This user guide is a collaborative effort on the part of ClinicalTrials.gov administrators at 11 academic medical centers around the nation to share efficient, best practices for most registrations based on our experience within our institutions. The recommendations within it should not be seen as necessarily required by law in all cases. The vast variety of circumstances for different registrations cannot be fully encompassed within a single slide set.

4 Tips and Recommendations Chrome and Firefox are more likely to let you expand text boxes to see more Use MS Word to create and edit these fields carefully Do not use first or second person. Replace I and we with the investigator ; replace you with participants Typos and spelling errors are not acceptable Define all acronyms Use notes provided by PRS system to guide you (suggestions/reminders; not mandatory) The Draft Receipt function provides a copy of your record as it appears in PRS

5 Validation Messages As you enter information, system validation (error, warning and note) messages may appear and disappear. Start by entering information for all required data elements. Note that some data elements are required, while others are conditionally required (based on information entered for other data elements). Finish by addressing all remaining validation messages. Complete all required fields before checking/stressing on validation.

6 Public Site

7 Protocol Registration and Results System Organization Name: WeillMC. To obtain a new ClinicalTrials.gov user account, please contact registerclinicaltrials@med.cornell.edu

8 To create a new record, click the New Record link or use the Records drop down menu The system flags records with problems to be addressed

9 This title will be displayed in search results IRB Protocol # Expanded Access records should only be created by the product manufacturer More explanations for this stage on next screen

10 The Help link contains examples and data entry tips The Definitions link contains the meaning of terms and useful information about field lengths

11 After you click Continue, you will see this dialog box Select OK

12 Required by ICMJE; should be consistent with formal IRB title Choose Quit to save work from previous screens, then Continue If the clinical study is funded in whole or in part by a U.S. Federal Government agency, the complete grant or contract number must be submitted as a Secondary ID. NIH grants should have an activity code (3 or 4 numbers and letters, such as R01), institute code (2 letters), and a 6 digit serial number. They may have a dash ( ) and suffix.

13 After you click Quit, you will see this dialog box Select OK

14 The Record Owner is the primary contact for the record. Only an administrator can change the Record Owner. PI can now share access with study team members and support staff PI is legally responsible for accuracy and veracity of the record, and for ensuring proper maintenance

15 Click Open to edit information section by section

16 As you fill in more information, the Record Summary will show your progress

17 Update this date every time the record is updated and review for accuracy. This is how compliance is tracked. Only use Active, not recruiting if data are still being collected. If data collection is complete, the status should be Completed or Terminated. Select Actual once date has occurred Select Anticipated for projections Save button is always at bottom of each page

18 Primary and Study Completion Dates Completion Dates are based on data collection They are NOT based on: data analysis database lock publication IRB closure If you use these as Completion Dates, you may have LATE RESULTS

19 Primary and Study Completion Dates Remember: Results for the primary outcome measure(s) are due within one year of the Primary Completion Date. Results for the secondary outcome measures are due one year after the completion date for that outcome. In this example, Primary Outcome results are due by September 15, All study results must be entered by March 15, Some secondary results may be due earlier depending on data collection time frames.

20 Choosing sponsor Responsible Party must be listed as Sponsor Sponsor should be Weill Medical College of Cornell University If the study is NIH funded, include the NIH Institute or Center as a Collaborator. Collaborators include other funders, etc. Add as many as necessary.

21 Refer to definitions and linked Checklist for these sections For Human Subjects Protections Review, provide the IRB information outlined in the WCM ClinicalTrials.gov Requirements for Posting. If this is Yes, the IND/IDE information is required You may leave this blank unless the protocol specifies if a data monitoring committee was established Neither of these questions is required. Section 801 Clinical Trial = ACT; FDAregulated intervention/section 801 clinical trial are optional; will likely eventually be phased out. We recommend NOT answering it unless your institution has a specific policy

22 Register before any enrollment begins. Provide the IRB information outlined in the WCM ClinicalTrials.gov Requirements for Posting.

23 Describe the study hypothesis in terms understandable to the lay public. It can be adapted from the informed consent, but omit any and all personal pronouns, (e.g. we, you). This field is optional and can be left blank. It does not have to be in lay language It can be adapted from the background or aims section of the protocol, but do not copy and paste the entire protocol. This field cannot contain promotional language. Where applicable, explain uncertainties or exploratory nature of study. If there are any parts of the trial, which the public cannot know about while the study is ongoing without affecting scientific integrity, such as deception research or inclusion/exclusion criteria which could be easily faked in order to join a study (e.g. pain levels in order to have access to a controlled substance), it would be good to explain here, e.g. Some inclusion/exclusion criteria are purposely omitted at this time to preserve scientific integrity. They will be included after the trial is complete.

24 Enter each study condition, one per line. Use Search MeSH link to verify the correct condition term Keywords help users find studies in the database

25 Check the definitions link Give an honest estimate for anticipated enrollment (based on consent, not completion)

26 Arms may not pre exist based on how many arms you defined in the previous section. You must add each arm. Do not title your arm as Intervention or Arm 1. Arm title should be more descriptive.

27 List Placebo as a Drug intervention Frequent PRS Comment: The preferred format is to include *all* interventions that were prespecified to be administered as part of the protocol, even if a particular intervention is not "of interest

28 Errors must be fixed to move on. Click edit to resolve these Errors Cross Reference tables will not exist for single arm studies. For multiple arm studies, you must link arms and interventions even when it seems that it s obvious that Arm A does intervention A and Arm B does intervention B.

29 Outcome Measures NEW! Protocol/statistical analysis plan must be submitted with results and will be public for studies with a primary completion date of 1/18/2017 or later Ensure coherence among protocol and registration for primary, secondary and other outcomes PRS reviewers may assume all outcomes are primary or secondary unless they are specified in the protocol as other or exploratory Include all PRIMARY and SECONDARY outcomes (tertiary/exploratory are optional) Label outcomes as primary or secondary per the protocol Can list more than one primary if applicable

30 Outcome Measures More registrations get rejected for inadequate Outcome Measure precision or inaccurate or multiple time frames than anything else. Outcome Measures should be specific and indicate what is being measured and is (or planned to be) reported. Remember the mantra: Outcome Measures must be measurable outcomes.

31 Outcome Measure Tips: Title Include the metric (i.e. scale, score, number, percentage) Ex: Safety Ex: Safety, as measured by number of subjects with at least one AE Be clear and concise; omit verbs Ex: To determine the maximum tolerated dose of Drug A in patients with breast cancer. Ex: Maximum Tolerated Dose of Drug A in patients with breast cancer List outcomes separately Ex: All cause mortality, hospitalizations, ER visits Ex: Number of hospitalizations, Number of ER visits, Number of ER visits. Should be listed as 3 separate outcomes Exception: if a composite score of multiple measures will be used Example: Count of individuals who experience any of the following: allcause mortality, hospitalizations, and emergency room visits

32 Outcome Measure Tips: Time Frame Be specific (e.g. # of minutes, weeks, months) Ex: Baseline, week 2 Ex: During hospitalization, approximately 5 days Ex: Post intervention, week 12 If multiple time points are included: If measuring change between the time points, add the word change to the title If not measuring change, each time point needs to be listed as a separate outcome measure Remember that completion dates should reflect completion of data collection for your outcome measures. Refer back to study status section. Average time, expected average time, or max assessment time would all be acceptable when the protocol cannot specify precise time frame

33 Outcome Measure Tips: Description If a scale will be used, include the range and meaning of the scores Example: The Hamilton Depression Rating Scale is used for rating the severity of depressive symptoms. Scores range from 0 to 50, with higher scores indicating greater severity of depression. If a scale is not linear (e.g. logarithmic), that would be good to note as well.

34 Outcome Measures: Example 1 There are 2 time points, so the word change is added to the title The Title includes the scale that will be used to assess change in pain The Description includes the range of the scale and what the scale means

35 Outcome Measures: Example 2 The title includes the metric The Time Frame includes the specific length of time The Description defines adverse events

36 Use Inclusion / Exclusion Criteria with colon followed by dashed list format No paragraphs Make sure that all criteria you post are appropriate for the public to see. Match informed consent more than protocol, if something might need to be masked from participants. If necessary, use Detailed Description field to flag that the eligibility criteria are deliberately incomplete to preserve the scientific integrity of the study

37 Add the PI as a Study Official

38 Overall contact may be used to differentiate a study coordinator or administrator from the study official. All sites should be added for multi site studies, only after the IRB has approved that location

39 Site recruitment status must be consistent with overall recruitment status; if overall recruitment is not recruiting, no site can be recruiting

40 Studies available in PubMed are linked automatically if the NCT# was included in the publication. Others need to be added manually Indicate if the reference provided reports results from this study

41 The Record Summary Click the Spelling link to review spelling errors and unexpanded acronyms Errors must be addressed before releasing the record Warnings indicate potentially serious issues that should be reviewed and addressed as needed Notes indicate other potential issues; address as needed When the Record Summary shows all green checks, the PI should carefully review the record. False statements are criminal under the regulations! For new registrations, the PI should read each section carefully

42 The Record Summary to complete Click Entry Complete to send the record to the Responsible Party for Approval and Release This study appears to be an ACT and is subject to federal regulations The reasons why your trial is considered ACT will be displayed

43 The Record Summary User Information The Record Owner is the primary contact for the record. Only an administrator can change the Record Owner Add the PI and anyone else who should have edit rights. The Record Owner can do this Initial Release date displays on the public site. This is important for FDAAA and ICMJE

44 Can a Study Record be Deleted? Only if the study record has never been published on ClinicalTrials.gov Otherwise, No. ClinicalTrials.gov serves as a long term public registry. Once a study record is published, it remains in the system even after a trial has closed. If you find a duplicate, contact ClinicalTrials.gov at register@clinicaltrials.gov.

45 PRS Review Once the record is released, ClinicalTrials.gov conducts a manual review If major issues are identified, the record owner and RP will receive notification from ClinicalTrials.gov with comments The study will be reset to In Progress Study Owner/RP must correct the issues and re release it within 15 calendar days (new in 42 CFR 11) If no major issues are identified, the study is assigned an NCT number and published on the public side of the database (clinicaltrials.gov) This process takes about 2 5 business days Even if its published, advisory comments may be posted. Corrections are not mandatory

46 Ongoing Responsibilities of Record Owners Records can be transferred to other user accounts as staff change Records must be updated every 12 months and within 30 days of Recruitment Status changes or amendments that affect information in clinicaltrials.gov record, especially recruitment status, location and contact information Always update the Record Verification Date to indicate that you have updated or reviewed the record Records must be updated within 30 days after the completion date (last data collection) Failure to update information on ClinicalTrials.gov can result in penalties. There are more specific update requirements in 42 CFR

47 Checking your Problem Records PRS System identifies current Problem Records Records that have not been marked as completed Active studies that have not been updated (or the Record Verification Date has not been updated) Records missing one or more FDAAA required data elements: Responsible Party Study Start Date Primary Completion Date Primary Outcome Measure Records that appear to be overdue for FDAAA results reporting

48 Do You Need to Submit Results? All Applicable Clinical Trials (ACTs) are required to submit results All NIH funded trials begun on after 1/18/2017 and applied for on or after 1/18/2017 must report results, whether ACTs or not Other grantors may require results submission Based on registration information entered, the system will assess whether the trial appears to be: 1) An ACT with results required by law 2) A Non ACT: results ARE not required by law, though NIH policy (if so funded) or other funders policies may still require results reporting 3) Older trials may be designated Probable ACT or Probable Non ACT Note: There is no reminder flag for NIH funded trials.

49 Acknowledgements This slide set was developed collaboratively by contributors from Beth Israel Deaconess Medical Center, Boston University Cambridge Health Alliance Duke University Fred Hutchinson Cancer Research Center Harvard University Mayo Clinic Partners Rutgers State University University of Michigan University of Pittsburgh University of South Florida Special thanks to: Isabel Chico Calero Niem Tzu Chen Melanie Chladny Wendy Duncan Patrick Fawcett Eleanor R. Greene Jessica Houlihan Odette Lobo Linda Mendelson Cynthia Monahan Carolyn Peterson Diane Wilson